All diseases

OMIM ID
256840
OMIM term:
NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE
Alternative terms:

(∗) Location:
5p15.2  
(†) Associated OMIM genes:
CCT5  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/t1qkguu3